Canonical Allele Identifier: CA1917771578

Gene: HK1

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.69382045_69382046delinsCT , CM000672.2:g.69382045_69382046delinsCT	GRCh38
NC_000010.10:g.71141801_71141802delinsCT , CM000672.1:g.71141801_71141802delinsCT	GRCh37
NC_000010.9:g.70811807_70811808delinsCT	NCBI36
NG_012077.1:g.117046_117047delinsCT , LRG_365:g.117046_117047delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000470050.2:c.1266-442_1266-441delinsCT	ENSP00000515580.1:n.1266-442_1266-441delinsCT
ENST00000703945.1:c.1182-442_1182-441delinsCT	ENSP00000515578.1:n.1182-442_1182-441delinsCT
ENST00000703946.1:c.1265+1950_1265+1951delinsCT	ENSP00000515579.1:n.1265+1950_1265+1951delinsCT
ENST00000703947.1:c.876-442_876-441delinsCT	ENSP00000515581.1:n.876-442_876-441delinsCT
ENST00000703948.1:c.*883-442_*883-441delinsCT	ENSP00000515582.1:n.*883-442_*883-441delinsCT
ENST00000703949.1:c.1266-442_1266-441delinsCT	ENSP00000515583.1:n.1266-442_1266-441delinsCT
ENST00000703950.1:c.1266-442_1266-441delinsCT	ENSP00000515584.1:n.1266-442_1266-441delinsCT
ENST00000703951.1:c.1265+1950_1265+1951delinsCT	ENSP00000515585.1:n.1265+1950_1265+1951delinsCT
ENST00000703952.1:c.1265+1950_1265+1951delinsCT	ENSP00000515586.1:n.1265+1950_1265+1951delinsCT
ENST00000703953.1:c.*529-442_*529-441delinsCT	ENSP00000515587.1:n.*529-442_*529-441delinsCT
ENST00000703954.1:c.1146-442_1146-441delinsCT	ENSP00000515588.1:n.1146-442_1146-441delinsCT
ENST00000703955.1:n.1816-442_1816-441delinsCT
ENST00000298649.8:c.1263-442_1263-441delinsCT	ENSP00000298649.3:n.1263-442_1263-441delinsCT
ENST00000359426.7:c.1266-442_1266-441delinsCT MANE Select	ENSP00000352398.6:n.1266-442_1266-441delinsCT
ENST00000436817.6:c.1278-442_1278-441delinsCT	ENSP00000415949.2:n.1278-442_1278-441delinsCT
ENST00000493591.6:c.*1154-442_*1154-441delinsCT	ENSP00000494917.1:n.*1154-442_*1154-441delinsCT
ENST00000643399.2:c.1278-442_1278-441delinsCT MANE Plus Clinical	ENSP00000494664.1:n.1278-442_1278-441delinsCT
ENST00000298649.7:c.1263-442_1263-441delinsCT	ENSP00000298649.3:n.1263-442_1263-441delinsCT
ENST00000359426.6:c.1266-442_1266-441delinsCT	ENSP00000352398.6:n.1266-442_1266-441delinsCT
ENST00000360289.6:c.1230-442_1230-441delinsCT	ENSP00000353433.2:n.1230-442_1230-441delinsCT
ENST00000448642.6:c.1278-442_1278-441delinsCT	ENSP00000402103.3:n.1278-442_1278-441delinsCT
ENST00000494253.1:n.1492-442_1492-441delinsCT
NM_000188.2:c.1266-442_1266-441delinsCT	NP_000179.2:n.1266-442_1266-441delinsCT
NM_033496.2:c.1263-442_1263-441delinsCT	NP_277031.1:n.1263-442_1263-441delinsCT
NM_033497.2:c.1278-442_1278-441delinsCT	NP_277032.1:n.1278-442_1278-441delinsCT
NM_033498.2:c.1278-442_1278-441delinsCT	NP_277033.1:n.1278-442_1278-441delinsCT
NM_033500.2:c.1230-442_1230-441delinsCT , LRG_365t1:c.1230-442_1230-441delinsCT	NP_277035.2:n.1230-442_1230-441delinsCT
XM_005269735.2:c.1395-442_1395-441delinsCT	XP_005269792.1:n.1395-442_1395-441delinsCT
XM_005269736.1:c.1278-442_1278-441delinsCT	XP_005269793.1:n.1278-442_1278-441delinsCT
XM_005269737.1:c.1182-442_1182-441delinsCT	XP_005269794.1:n.1182-442_1182-441delinsCT
XM_011539732.1:c.1230-442_1230-441delinsCT	XP_011538034.1:n.1230-442_1230-441delinsCT
XM_011539733.1:c.1224-442_1224-441delinsCT	XP_011538035.1:n.1224-442_1224-441delinsCT
XM_011539734.1:c.1221-442_1221-441delinsCT	XP_011538036.1:n.1221-442_1221-441delinsCT
NM_001322364.1:c.1278-442_1278-441delinsCT	NP_001309293.1:n.1278-442_1278-441delinsCT
NM_001322365.1:c.1371-442_1371-441delinsCT	NP_001309294.1:n.1371-442_1371-441delinsCT
NM_001322366.1:c.1182-442_1182-441delinsCT	NP_001309295.1:n.1182-442_1182-441delinsCT
NM_001322367.1:c.1170-442_1170-441delinsCT	NP_001309296.1:n.1170-442_1170-441delinsCT
NM_001358263.1:c.1278-442_1278-441delinsCT MANE Plus Clinical	NP_001345192.1:n.1278-442_1278-441delinsCT
XM_024447969.1:c.1278-442_1278-441delinsCT	XP_024303737.1:n.1278-442_1278-441delinsCT
NM_000188.3:c.1266-442_1266-441delinsCT MANE Select	NP_000179.2:n.1266-442_1266-441delinsCT
NM_001322364.2:c.1278-442_1278-441delinsCT	NP_001309293.1:n.1278-442_1278-441delinsCT
NM_001322365.2:c.1371-442_1371-441delinsCT	NP_001309294.1:n.1371-442_1371-441delinsCT
NM_033496.3:c.1263-442_1263-441delinsCT	NP_277031.1:n.1263-442_1263-441delinsCT
NM_033497.3:c.1278-442_1278-441delinsCT	NP_277032.1:n.1278-442_1278-441delinsCT
NM_033498.3:c.1278-442_1278-441delinsCT	NP_277033.1:n.1278-442_1278-441delinsCT